FDA Registration
Active
🇺🇸 United States
Penumbra System (Reperfusion Catheter RED 72)
Reg #: 3013758550
·
FEI: 3013758550
·
Expires 2025
Products
1
Proprietary Names
1
Establishment Types
1
Classifications
1
Registration Details
- Registration Name
- Penumbra Inc.
- Registration Number
- 3013758550
- FEI Number
- 3013758550
- Status
- Active
- Expiry Year
- 2025
- Initial Importer
- No
- Address
- 6262 Patterson Pass Rd,, Suite A, Suite E, Suite F, 6336 Patterson Pass Rd, Suite D
- City
- Livermore
- State
- CA
- ZIP
- 94550
- Country
- US
Regulatory Submissions
- 510(k) Number
- K211654
Owner / Operator
- Firm Name
- PENUMBRA, INC.
- Operator Number
- 9072336
- Address
- One Penumbra Place
- City
- Alameda
- State
- CA
- Postal Code
- 94502
- Country
- US
Products
| Device Name | Product Code | Device Class | Medical Specialty | Exempt | Created |
|---|---|---|---|---|---|
| Catheter, Thrombus Retriever | NRY | Class 2 | Cardiovascular | No | 2021-08-19 |
Proprietary Names
Penumbra System (Reperfusion Catheter RED 72)
Establishment Types
Manufacture Medical Device